1,698 Results for

Director Of Quality Jobs in San Jose, CA

Jobs

New!

Palo Alto, CAToday

$1,956–$1,956

Advantis Medical, the #1 rated travel nurse agency, is currently seeking an experienced Director of Nursing Registered Nurse (RN) for an exciting new travel job in Palo Alto, CA 94303. If you are an experienced Director of Nursing Registered Nurse (RN) with a passion for providing exceptional patient care, just let us know you’re interested.

New!

Pleasanton, CAToday

$2,337–$2,337

Advantis Medical, the #1 rated travel nurse agency, is currently seeking an experienced Director of Nursing Registered Nurse (RN) for an exciting new travel job in Pleasanton, CA 94588. If you are an experienced Director of Nursing Registered Nurse (RN) with a passion for providing exceptional patient care, just let us know you’re interested.

New!

Santa Clara, CA3 days ago

$225,000–$300,000 Per Year

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San Jose, CA17 days ago

$145–$159 Per Hour
Full-time

We are seeking an experienced hospitalist with leadership capabilities for Regional Medical Center, a thriving hospitalist program located in the heart of tech mecca, San Jose, California. Competitive Compensation, with an estimated base salary range of $145 to $159 hourly, RVU and quality bonus, plus leadership stipend, with the opportunity to earn additional incentives.

Burlingame, CA12 days ago

Sutter Mills-Peninsula Medical Center earned five stars, the highest ranking possible, in the CMS Overall Hospital Quality Star Ratings and an Outstanding Patient Experience Award, placing it among the top 15 percent of hospitals in patient experience. Ensure practice is appropriately represented and demonstrates their value through leadership roles (as applicable) and/or participation with hospital management, medical staff leadership, Medical Executive, Medical Staff and other hospital committees, and within the local community.

New!

Redwood City, CAToday

Ensure practice is appropriately represented and demonstrates their value through leadership roles (as applicable) and/or participation with hospital management, medical staff leadership, Medical Executive, Medical Staff and other hospital committees, and within the local community. Strategize and execute a comprehensive annual practice management plan that sets clear goals and objectives, continuously surpassing expectations and delivering value to patients, clients, providers, and the local community.

San Jose, CA12 days ago

$139,256–$222,768

Our infrastructure includes a fullyautomated esoteric core laboratory in Fort Lauderdale, a histology and microbiology operation in Largo,Florida, and a network of hospital based rapid-response laboratories present in fourHCA Healthcare divisions within the state of Florida. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.

San Leandro, CA22 days ago

$116,000–$147,000 Per Year

Kindred Hospital San Francisco Bay Area is a 99-bed long-term acute care hospital offering the same in-depth care you would receive in a traditional hospital, but for an extended recovery period. Maintains oversight responsibility for all regulatory body surveys, including The Joint Commission (TJC), State Licensing Reviews, and CMS Validation surveys.

Pleasanton, CA30+ days ago

10+ years of relevant regulatory affairs experience in the bioanalytical CRO or biotechnology/pharmaceutical industry, or a combination of education and experience. Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading biologics analytical organization with operations in the San Francisco Bay Area and New Jersey.

Santa Clara, CA30+ days ago

This is a high-impact technical leadership role perfect for a hands-on seasoned QE leader who has experience running large quality engineering and tool development organizations. Oversee the long term testing / pre-production environment strategy, ensuring high availability and stability for testing environments used by the entire company.

San Jose, CA30+ days ago

$192,000–$210,000 Per Year

Data and Metrics Governance • Understand and support existing key performance indicators (KPIs) and quality metrics to ensure process improvements align with organizational objectives • Assess impact of proposed system and data changes on established governance frameworks and data integrity • Collaborate with data governance teams to evaluate risks and opportunities related to metrics and reporting when implementing process changes • Analyze performance data to identify trends, opportunities, and areas for improvement while maintaining alignment with existing measurement systems. • Model: Operational Excellence Focus • Location: San Francisco Bay Area preferred; other northern California locations considered • Success Metrics • Successful implementation of quality improvement initiatives • Measurable improvements in operational KPIs and process efficiency • Effective stakeholder engagement and cross-functional collaboration • Timely completion of assigned projects and deliverables • Knowledge transfer and capability building within client organization.

san jose, CA30+ days ago

$140,000–$165,000 Per Year

Oversight of managing and improving site supplier quality Be an advocate for lean and six sigma manufacturing principles and drive continuous improvement Drive cross functional projects with manufacturing, supply chain, and engineering to verify and validate existing manufacturing processes and capabilities Coordinate development of Quality Plan and participate in Design for Manufacturability (DFM) reviews for new customer on-boarding Address process yields by driving cross-functional teams to develop and implement corrective actions utilizing a methodical approach (DMAIC) to root cause and continuous improvement. Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors.

San Jose, California30+ days ago

$190,000–$230,000 Per Year

Driven by a belief that infectious disease diagnosis should be quick, accurate, and accessible to all, Visby has developed the world’s first single-use PCR platform that disrupts the traditional model and redefines the way infectious disease is tested and treated.$190,000 You will lead and participate in all aspects of the quality management system (QMS) and work closely with cross-functional teams to drive continuous improvement and maintain compliance with the QMS throughout the product lifecycle.

Sunnyvale, CA16 days ago

$200,000–$230,000 Per Year

A Director of Quality Management who excels in this role: Provides leadership and oversight of a comprehensive, efficient and integrated organization wide Continuous Quality Performance Improvement program. We are part of Lifepoint Health, a diversified healthcare delivery network committed to making communities healthier with acute care, rehabilitation, and behavioral health facilities from coast to coast.

Alameda, California30+ days ago

$210,000–$250,000 Per Year

GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies. A minimum of 15 years of experience in compliance, quality, and CDMO/CMO management with a focus on regulatory documentation and lifecycle management within the pharmaceutical or biotechnology industry is a must, including 10 years of experience in management/leadership roles.

New!

Palo Alto, California3 days ago

HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. The Senior Director QA will report to the Vice President, Quality Assurance and Regulatory CMC, and provide comprehensive GMP quality oversight across the full chemistry, manufacturing, and controls (CMC) lifecycle for Summit’s oncology pipeline.

Palo Alto, CA24 days ago

$217,000–$271,000 Per Year

HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. Overview of Role: The Senior Director QA will report to the Vice President, Quality Assurance and Regulatory CMC, and provide comprehensive GMP quality oversight across the full chemistry, manufacturing, and controls (CMC) lifecycle for Summit's oncology pipeline.

New!

San Mateo, CA2 days ago

Work with QA/QC responsible person and the Project Executive to compile checklist of hot points applicable to assigned projects (Glazing, EIFS, Roofing System, Wall Systems, Water Proofing, Sealants, Metal Panel Systems, and Swimming Pools). Management of Quality Assurance/Quality Control Staff Work in conjunction with the regional Operations Manager in conducting annual performance reviews for QA/QC personnel establishing meaningful goals and an accurate reflection of their performance.

New!

Menlo Park, CA3 days ago

Remote

Antheia is seeking an experienced and driven Associate Director of Global Quality to provide hands-on quality leadership across our regulated starting material (RSM) and pharmaceutical active pharmaceutical ingredient (API) operations. Maintain current knowledge of evolving GMP regulations, ICH guidelines, and DEA requirements relevant to controlled substance API and RSM manufacturing; communicate changes and impact assessments to leadership.

South San Francisco, CA30+ days ago

$205,000–$218,000 Per Year

We work hard to bring together diverse teams-grounded in a wide range of expertise and life experiences-and work even harder to ensure those teams thrive in inclusive, growth-oriented environments supported by equitable company and team practices. These powerful models rely on extensive biological and computational infrastructure and allow insitro to advance novel targets and patient biomarkers, design therapeutics and inform clinical strategy.

South San Francisco, CA30+ days ago

$184,500–$215,250 Per Year

This role will hare strategic responsibility for the QA CSV / CSA function to support cross-functional and QA goals for GXP systems and deliver results for corporate initiatives, as well as independently drive and own multiple complex CSV-related projects in partnership with multiple cross-functional leaders. Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.

Sunnyvale, CA30+ days ago

$115,900–$141,700 Per Year

As a Director of Quality Management, your responsibilities will include: Initiate and manage key projects for product quality improvement, such as reducing cost of quality, product RMA rate and IQC failure rate, increasing production yield rate etc…; closely drive and track them to completion with all targets achieved. Strong people management experience and skill to assess and utilize existing team's skill sets and capabilities to support business needs, and to hire, coach, mentor new team members for business expansion.

San Jose, CA25 days ago

$170,700–$256,100 Per Year

Lyten is leading an industrial revolution through Lyten 3D Graphene, a breakthrough supermaterial unlocking a new generation of products - from lithium-sulfur batteries and energy storage systems to concrete admixtures, lightweight composites, and next-generation sensors that are revolutionizing industries. Doctorate degree in engineering or general sciences AND 12+ years of experience in Quality OR Master's degree in engineering or general sciences AND 14+ years of experience in Quality OR Bachelor's degree in engineering or general sciences AND 16+ years of experience in Quality OR equivalent experience.

San Jose, California27 days ago

Lyten is leading an industrial revolution through Lyten 3D Graphene, a breakthrough supermaterial unlocking a new generation of products — from lithium–sulfur batteries and energy storage systems to concrete admixtures, lightweight composites, and next-generation sensors that are revolutionizing industries. Doctorate degree in engineering or general sciences AND 12+ years of experience in Quality OR Master's degree in engineering or general sciences AND 14+ years of experience in Quality OR Bachelor's degree in engineering or general sciences AND 16+ years of experience in Quality OR equivalent experience.

Menlo Park, CA16 days ago

$213,000–$240,000 Per Year

Role Overview: The Director, Quality Control - Combination Products will provide strategic and operational leadership for the Quality Control function supporting late-stage clinical development, analytical testing oversight for clinical drug substance and drug product, process performance qualification (PPQ), regulatory submissions, and commercial launch readiness for monoclonal antibody drug products and combination products, including pre-filled syringes and autoinjectors. Strong knowledge of cGMP regulations and global regulatory expectations, including 21 CFR Parts 210, 211, and 4. Hands-on experience supporting combination products such as pre-filled syringes, autoinjectors, or related delivery systems.

San Jose, CA19 days ago

Oversee the harmonization of quality system processes at various global sites included in the scope of the Invisalign quality system including internal audits, document control, risk management, non-conformance and corrective action handling, inspections, training, and management review. The successful candidate will partner with Align Global QMS leaders to create a quality management infrastructure that is compliant, effective, efficient, agile, and that supports a rapidly growing business with complex and diverse product lines (both hardware and software).

New!

San Mateo, CA2 days ago

$190,000–$205,000 Per Year

Oversee system configuration, user acceptance testing (UAT), and validation activities (e.g., CSV/CSA) to ensure the system is fit for intended use and compliant with global GMP regulations. Demonstrated ability to successfully interact with regulatory health authorities at inspections and thorough understanding of audit and vendor management programs.

South San Francisco, CA11 days ago

$200,000–$270,000 Per Year

By offering trust, flexibility, and autonomy through programs like NovoLife, our flexible benefits framework, we empower team members to create an effective work-life balance that delivers professional satisfaction and maximum results for clients. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of the industry with an award-winning workplace culture that values ambition, innovation, and growth.

San Jose, CA30+ days ago

$225,700–$326,800 Per Year

Adobe's industry-leading offerings including Adobe Acrobat Studio, Adobe Express, Adobe Firefly, Creative Cloud, Adobe Experience Platform, Adobe Experience Manager, and GenStudio enable people and businesses to turn ideas into impact, powered by AI and driven by human ingenuity. Learn more about Adobe life, including our values and culture, focus on people, purpose and community, Adobe for All, comprehensive benefits programs, the stories we tell, the customers we serve, and how you can help us advance our mission of empowering everyone to create.

South San Francisco, CA30+ days ago

$193,638–$224,270 Per Year

The Associate Director, GCP Clinical Quality will play a key role in ensuring the successful execution of Denali's clinical trials by delivering strategic quality oversight and fostering a culture of compliance and continuous improvement. Key Accountabilities/Core Job Responsibilities: Serve as a GCP Quality team member on Study Execution Teams (SETs) and deliver a cohesive strategic GCP framework across Denali clinical trials.

Brisbane, CA30+ days ago

$170,538–$193,493 Per Year

As a virtual drug developer, Nurix operates through a lean internal infrastructure and relies on a curated ecosystem of Software-as-a-Service (SaaS) and cloud-hosted platforms to support GxP-regulated activities across clinical development, quality operations, manufacturing oversight, and regulatory submissions. The role requires an individual who combines deep technical knowledge of GxP computerized systems with practical experience in SaaS and cloud-based platform qualification, and who can translate regulatory requirements into pragmatic, fit-for-purpose validation approaches that support a modern, agile biotech environment.

South San Francisco, CA10 days ago

$192,000–$249,000 Per Year

Key Accountabilities/Core Job Responsibilities: Oversee GMP and GLP quality operations at CMOs, including quality documentation reviews and approvals, from Manufacturing and Quality Control, such as batch records, change controls and specifications, disposition of Denali products and audits as needed. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.

New!

San Carlos, California3 days ago

$300,000–$350,000 Per Year

The Executive Director, Quality Assurance, External Manufacturing is responsible for leading the External Manufacturing Quality function and executing the quality strategy across Vaxcyte’s global network of Contract Development and Manufacturing Organizations (CDMOs) and external partners. This leader drives a proactive, risk-based quality approach and implements scalable systems, governance, and partnerships to enable operational excellence across the external network, supporting clinical development, BLA readiness, and commercial supply.

Redwood City, CA30+ days ago

Lead, manage, and train others on GCP audits, including clinical investigative site audits, clinical vendor audits, clinical department internal audits, Trial Master File (TMF) audits, and applicable study document audits, including Clinical Study Reports (CSRs). The Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept.

Foster City, CA30+ days ago

$190,000–$205,000 Per Year

10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality and 5+ years supervising GCP Quality internal staff and/or external consultants. Provide quality oversight for the GCP/GVP/GLP vendor activities, including internal/external deviations, CAPAs, change controls, and KPIs/KQIs.

Santa Clara, CA30+ days ago

Act as the voice of the customer, addressing complaints, ensuring needs are met, and be the key contact point for supporting complex and high impact quality-related issues with potential for considerable impact to the business. We are looking for a Senior Director of Customer Quality Engineer in a leadership role to support lead our customer quality assurance activities, stationed in Santa Clara, California!

New!

Foster City, California3 days ago

Provide quality oversite for the GCP/GVP/GLP vendor activities, including internal/external deviations, CAPAs, change controls, and KPIs/KQIs. 10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality and 5+ years supervising GCP Quality internal staff and/or external consultants.

Foster City, CA30+ days ago

$197,129–$221,404 Per Year

Oversee system configuration, user acceptance testing (UAT), and validation activities (e.g., CSV/CSA) to ensure the system is fit for intended use and compliant with global GMP regulations. Knowledge, Skills and Abilities: 12+ years' experience and strong background in Quality and Quality Systems in the drug development industry with knowledge of cGMP/ICH/FDA/EMA regulations.

New!

San Jose, CA2 days ago

Manage the activities of the technical documentation function including engineering/manufacturing SOP documentation, drawings, Bills of Materials, parts list, specifications, and engineering change orders. Release new, change existing, obsolete old, and distribute soft copies of controlled documents to Suppliers and CMs .

Fremont, California29 days ago

$155,000–$200,000

This role ensures effective implementation of the Bionova Quality Management System, supports delivery of a state-of-the-art, automated laboratory in collaboration with Engineering, and works cross-functionally and with clients to ensure timely, reliable, and regulatory-compliant analytical results. This role requires deep expertise in Quality Control operations and quality systems, along with demonstrated leadership capability and the ability to effectively influence teams and stakeholders across organizational and global environments.

Fremont, California29 days ago

$155,000–$200,000

South San Francisco, CA30+ days ago

$232,000–$271,000 Per Year

The Associate Director, Analytical Development and Quality Control will report to the Director & Head of Analytical Development and Quality Control and will be responsible for providing and executing analytical development strategy for small-molecule candidates from early development through late stage, including analytical method development, validation, and transfer; stability programs; and phase-appropriate specifications and analytical control strategies for drug substance (DS), drug product (DP), and related critical materials. Demonstrated track record of managing CROs and CDMOs, preferably on both analytical and bioanalytical projects, in developing methods and quality control strategy for testing of small-molecule drug candidates supporting Phase I to commercial launch.

New!

South San Francisco, CA5 days ago

$215,600–$266,300 Per Year

The Director, CMC QA will report to the Senior Director of CMC QA and be responsible for maintaining strategic responsibility over QA Manufacturing Operations, developing and implementing Ultragenyx CMC Quality approach for assigned programs, and working with colleagues to improve processes utilized to ensure product quality. In this role, in collaboration with key stakeholders in Technical Operations, DIR CMC QA provides quality oversight and support to ensure clinical through commercial development lifecycle activities for drug substance and drug product meet cGMP regulatory requirements and guidelines.

San Mateo, California18 days ago

Remote

Active, unrestricted licensure as an Advanced Practice Provider (Nurse Practitioner, Physician Assistant, Clinical Nurse Specialist, or equivalent) and willingness to obtain additional state licensure upon hire. The Clinical Director of Training & Quality is a senior leadership role responsible for designing, implementing, and continuously improving the education, quality, and accreditation programs that underpin our value-based, home-based Palliative Care model.

South San Francisco, CA9 days ago

$230,000–$270,000 Per Year

Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease.

South San Francisco, CA30+ days ago

$230,000–$270,000 Per Year

Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease.

Menlo Park, CA16 days ago

$213,000–$240,000 Per Year

Review and approve GMP documentation, including master batch records, executed batch records, analytical methods, specifications, validation protocols and reports, tech transfer documentation, stability protocols and reports, and risk-assessment documentation. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year.

South San Francisco, CA30+ days ago

$193,000–$242,000 Per Year

The Clinical QA Director is responsible to ensure quality is embedded throughout the lifecycle of all the ongoing clinical programs through oversight, assessment and monitoring, risk assessment tools, auditing and risk mitigations. This involves working closely with Clinical Operations, Clinical Development, Clinical Supply Chain, Data Management, Pharmacovigilance, Medical Affairs, Regulatory, Legal, and other teams across Alumis.

Redwood City, California30+ days ago

The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Collaborate cross-functionally with teams in drug substance, drug product, supply chain, quality, regulatory, sourcing and other related team to ensure alignment of stability design and achieve stability study objectives.

Fremont, California29 days ago

$155,000–$200,000

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Director Of Quality Jobs in San Jose, CA

Travel Nurse RN - Director of Nursing - $1,956 per week in Palo Alto, CA TravelNurseSource

Travel Nurse RN - Director of Nursing - $2,337 per week in Pleasanton, CA TravelNurseSource

Tax Director Jobot

Hospitalist Assistant Medical Director in San Jose, CA TeamHealth

Medical Director - Psychiatry - Mills-Peninsula Medical Center Vituity

Medical Director Correctional Health - San Mateo County Jail Vituity

Hospital Laboratory Director Good Samaritan Hospital

Director of Quality Management Full Time Knight Health Holdings LLC

Manager/ Director of Quality Assurance CRYSTAL PHARMATECH INC

Director of Quality Engineering Netskope Inc

Senior Director of Quality Assurance Jones Lang LaSalle Inc

Regional Director of Quality Engineering Sanmina Corp

Director of Quality Visby Medical

Director of Quality Management (DQM) LifePoint Health Inc

Director of Quality Assurance GeneFab

Senior Director of Technical QA (GMP) Summit Therapeutics

Senior Director of Technical QA GMP Summit Therapeutics Inc

Director of Safety and Quality in Construction s j amoroso construction

Associate Director of Global Quality Antheia

Director, Quality Assurance Insitro Inc

Associate Director, QA Computer System Validation Cytokinetics Inc

Director, Quality Management Fortinet Inc

Sr Director, Quality Lyten Inc

Sr Director, Quality Lyten

Director, Quality Control Oruka Therapeutics Inc

Director, Quality Systems Align Technology, Inc.

Associate Director, Quality System, QMS Mirum Pharmaceuticals

Senior Director Quality Assurance Novotech Health Holdings Pte Ltd

Director, Engineering Operations (Chief of Staff to VP of Engineering, Adobe Express) ADOBE Inc

Associate Director, Clinical Quality Denali Therapeutics Inc

Associate Director, Computer Systems Assurance Quality Nurix Therapeutics Inc

Director, Quality (QA/QC) Denali Therapeutics Inc

Executive Director Quality Assurance, External Manufacturing Vaxcyte

Director, Clinical Quality Assurance Corcept Therapeutics Inc

Associate Director, GCP QA Mirum Pharmaceuticals Inc

Senior Director, Customer Quality Engineering NVIDIA Corp

Associate Director, GCP QA Mirum Pharmaceuticals

Associate Director, Quality System, QMS Mirum Pharmaceuticals Inc

Director Quality Management Systems Sakuu

Sr Manager/AD/Director of QC Veloxis Pharmaceuticals

Sr Manager/AD/Director of QC Asahi Kasei Plastics North America, Inc.

Associate Director, Analytical Development and Quality Control Aligos Therapeutics Inc

Director External Quality Assurance Ultragenyx Pharmaceutical Inc

Clinical Director, Training & Quality Vynca

Senior Director, Validation and Quality Engineering Allogene Therapeutics

Senior Director, Validation and Quality Engineering Allogene Therapeutics Inc

Director, GMP Quality Assurance Oruka Therapeutics Inc

Director, Clinical Quality Assurance - Contractor Alumis Inc

Director, Stability Management, Analytical Development and Quality Control Revolution Medicines

Sr Manager/AD/Director of QC Bionique Testing Laboratories LLC

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